Canonical Allele Identifier: CA351050321

Gene: SAG

Linked Data

• MyVariant Identifiers: chr2:g.234255486T>A (hg19) ; chr2:g.233346840T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.233346840T>A , CM000664.2:g.233346840T>A	GRCh38
NC_000002.11:g.234255486T>A , CM000664.1:g.234255486T>A	GRCh37
NC_000002.10:g.233920225T>A	NCBI36
NG_009116.1:g.44178T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000409110.6:c.1146T>A MANE Select	ENSP00000386444.1:p.Phe382Leu
ENST00000409110.5:c.1146T>A	ENSP00000386444.1:p.Phe382Leu
ENST00000412969.6:n.2366T>A
ENST00000471884.5:n.3177T>A
ENST00000474220.5:n.352T>A
ENST00000476500.5:n.6445T>A
ENST00000492629.1:n.107T>A
NM_000541.4:c.1146T>A	NP_000532.2:p.Phe382Leu
XM_011511589.1:c.1146T>A	XP_011509891.1:p.Phe382Leu
XM_011511590.1:c.1146T>A	XP_011509892.1:p.Phe382Leu
XM_011511591.1:c.*14T>A	XP_011509893.1:n.*14T>A
XM_011511592.1:c.990T>A	XP_011509894.1:p.Phe330Leu
XM_011511593.1:c.846T>A	XP_011509895.1:p.Phe282Leu
XM_011511594.1:c.774T>A	XP_011509896.1:p.Phe258Leu
XM_011511596.1:c.744T>A	XP_011509898.1:p.Phe248Leu
XM_011511597.1:c.744T>A	XP_011509899.1:p.Phe248Leu
XR_922978.1:n.1463T>A
XR_922979.1:n.1467T>A
XR_922980.1:n.1562T>A
XM_011511593.3:c.846T>A	XP_011509895.1:p.Phe282Leu
XM_017004641.1:c.*14T>A	XP_016860130.1:n.*14T>A
XM_024453036.1:c.*14T>A	XP_024308804.1:n.*14T>A
XR_001738882.1:n.1344T>A
XR_922980.2:n.1562T>A
NM_000541.5:c.1146T>A MANE Select	NP_000532.2:p.Phe382Leu